Cargando…
Distinct Roles for KASH Proteins SINE1 and SINE2 in Guard Cell Actin Reorganization, Calcium Oscillations, and Vacuolar Remodeling
The linker of nucleoskeleton and cytoskeleton (LINC) complex is a protein complex spanning the inner and outer membranes of the nuclear envelope. Outer nuclear membrane KASH proteins interact in the nuclear envelope lumen with inner nuclear membrane SUN proteins. The paralogous Arabidopsis KASH prot...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9120628/ https://www.ncbi.nlm.nih.gov/pubmed/35599883 http://dx.doi.org/10.3389/fpls.2022.784342 |
_version_ | 1784710970851983360 |
---|---|
author | Biel, Alecia Moser, Morgan Groves, Norman R. Meier, Iris |
author_facet | Biel, Alecia Moser, Morgan Groves, Norman R. Meier, Iris |
author_sort | Biel, Alecia |
collection | PubMed |
description | The linker of nucleoskeleton and cytoskeleton (LINC) complex is a protein complex spanning the inner and outer membranes of the nuclear envelope. Outer nuclear membrane KASH proteins interact in the nuclear envelope lumen with inner nuclear membrane SUN proteins. The paralogous Arabidopsis KASH proteins SINE1 and SINE2 function during stomatal dynamics induced by light–dark transitions and ABA. Previous studies have shown F-actin organization, cytoplasmic calcium (Ca(2+)) oscillations, and vacuolar morphology changes are involved in ABA-induced stomatal closure. Here, we show that SINE1 and SINE2 are both required for actin pattern changes during ABA-induced stomatal closure, but influence different, temporally distinguishable steps. External Ca(2+) partially overrides the mutant defects. ABA-induced cytoplasmic Ca(2+) oscillations are diminished in sine2-1 but not sine1-1, and this defect can be rescued by both exogenous Ca(2+) and F-actin depolymerization. We show first evidence for nuclear Ca(2+) oscillations during ABA-induced stomatal closure, which are disrupted in sine2-1. Vacuolar fragmentation is impaired in both mutants and is partially rescued by F-actin depolymerization. Together, these data indicate distinct roles for SINE1 and SINE2 upstream of this network of players involved in ABA-based stomatal closure, suggesting a role for the nuclear surface in guard cell ABA signaling. |
format | Online Article Text |
id | pubmed-9120628 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-91206282022-05-21 Distinct Roles for KASH Proteins SINE1 and SINE2 in Guard Cell Actin Reorganization, Calcium Oscillations, and Vacuolar Remodeling Biel, Alecia Moser, Morgan Groves, Norman R. Meier, Iris Front Plant Sci Plant Science The linker of nucleoskeleton and cytoskeleton (LINC) complex is a protein complex spanning the inner and outer membranes of the nuclear envelope. Outer nuclear membrane KASH proteins interact in the nuclear envelope lumen with inner nuclear membrane SUN proteins. The paralogous Arabidopsis KASH proteins SINE1 and SINE2 function during stomatal dynamics induced by light–dark transitions and ABA. Previous studies have shown F-actin organization, cytoplasmic calcium (Ca(2+)) oscillations, and vacuolar morphology changes are involved in ABA-induced stomatal closure. Here, we show that SINE1 and SINE2 are both required for actin pattern changes during ABA-induced stomatal closure, but influence different, temporally distinguishable steps. External Ca(2+) partially overrides the mutant defects. ABA-induced cytoplasmic Ca(2+) oscillations are diminished in sine2-1 but not sine1-1, and this defect can be rescued by both exogenous Ca(2+) and F-actin depolymerization. We show first evidence for nuclear Ca(2+) oscillations during ABA-induced stomatal closure, which are disrupted in sine2-1. Vacuolar fragmentation is impaired in both mutants and is partially rescued by F-actin depolymerization. Together, these data indicate distinct roles for SINE1 and SINE2 upstream of this network of players involved in ABA-based stomatal closure, suggesting a role for the nuclear surface in guard cell ABA signaling. Frontiers Media S.A. 2022-05-06 /pmc/articles/PMC9120628/ /pubmed/35599883 http://dx.doi.org/10.3389/fpls.2022.784342 Text en Copyright © 2022 Biel, Moser, Groves and Meier. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Plant Science Biel, Alecia Moser, Morgan Groves, Norman R. Meier, Iris Distinct Roles for KASH Proteins SINE1 and SINE2 in Guard Cell Actin Reorganization, Calcium Oscillations, and Vacuolar Remodeling |
title | Distinct Roles for KASH Proteins SINE1 and SINE2 in Guard Cell Actin Reorganization, Calcium Oscillations, and Vacuolar Remodeling |
title_full | Distinct Roles for KASH Proteins SINE1 and SINE2 in Guard Cell Actin Reorganization, Calcium Oscillations, and Vacuolar Remodeling |
title_fullStr | Distinct Roles for KASH Proteins SINE1 and SINE2 in Guard Cell Actin Reorganization, Calcium Oscillations, and Vacuolar Remodeling |
title_full_unstemmed | Distinct Roles for KASH Proteins SINE1 and SINE2 in Guard Cell Actin Reorganization, Calcium Oscillations, and Vacuolar Remodeling |
title_short | Distinct Roles for KASH Proteins SINE1 and SINE2 in Guard Cell Actin Reorganization, Calcium Oscillations, and Vacuolar Remodeling |
title_sort | distinct roles for kash proteins sine1 and sine2 in guard cell actin reorganization, calcium oscillations, and vacuolar remodeling |
topic | Plant Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9120628/ https://www.ncbi.nlm.nih.gov/pubmed/35599883 http://dx.doi.org/10.3389/fpls.2022.784342 |
work_keys_str_mv | AT bielalecia distinctrolesforkashproteinssine1andsine2inguardcellactinreorganizationcalciumoscillationsandvacuolarremodeling AT mosermorgan distinctrolesforkashproteinssine1andsine2inguardcellactinreorganizationcalciumoscillationsandvacuolarremodeling AT grovesnormanr distinctrolesforkashproteinssine1andsine2inguardcellactinreorganizationcalciumoscillationsandvacuolarremodeling AT meieriris distinctrolesforkashproteinssine1andsine2inguardcellactinreorganizationcalciumoscillationsandvacuolarremodeling |